Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Aidapak Services is recalling Carbidopa/Levodopa tablets that may have been mislabeled as Digoxin. Patients should verify their medication labels.
Aidapak Services, LLC is recalling Losartan Potassium 50 mg tablets because they may have been mislabeled as Midodrine HCL 2.5 mg.
Aidapak Services, LLC is recalling 923 tablets of Cyanocobalamin 1000 mcg because they may have been mislabeled as other medications.
Aidapak Services, LLC is recalling 2 mg Nicotine Polacrilex Gum due to a potential labeling mixup with Folic Acid or Quetiapine Fumarate tablets.
Aidapak Services is recalling 10 mg Fosinopril Sodium tablets that may be mislabeled as Mercaptopurine 50 mg.
Aidapak Services is recalling Mycophenolate Mofetil capsules because they may have been mislabeled as Atorvastatin or Propranolol.
Aidapak Services is recalling Losartan Potassium 50 mg tablets because they may have been mislabeled as Atorvastatin Calcium 80 mg.
Aidapak Services, LLC is recalling Triamterene/HCTZ tablets that may have been mislabeled as Caffeine tablets. The error involves a label mixup during repacking.
KVK-Tech, Inc. is recalling 14,664 bottles of Hydroxyzine Hydrochloride 10 mg tablets because the active ingredient came from an unapproved source.
Aidapak Services is recalling Verapamil HCL tablets because they may have been mislabeled as Atorvastatin or Tacrolimus.
Aidapak Services, LLC is recalling Nortriptyline HCL capsules because they may have been mislabeled as other medications. The affected drugs were distributed in four western states.
Aidapak Services, LLC is recalling CapsuleTOPRIL tablets because they may have been mislabeled as Calcitriol capsules. The error could lead to patients receiving the wrong medication.
Aidapak Services, LLC is recalling 5 mcg Liothyronine Sodium tablets because they may have been mislabeled as 25 mcg tablets.
Aidapak Services, LLC is recalling Dronedarone HCL 400 mg tablets because they may be mislabeled as Methylergonovine Maleate 0.2 mg.
Aidapak Services is recalling Repaglinide 1 mg tablets because they may have been mislabeled as Valsartan, Guaifenesin, or Magnesium Chloride.
Aidapak Services, LLC is recalling Propranolol HCL ER capsules because they may have been mislabeled as Cinacalcet HCL tablets.
Aidapak Services, LLC is recalling Oxybutynin Chloride 5 mg tablets because they may have been mislabeled as other prescription drugs.
Aidapak Services is recalling Nefazodone HCL 150 mg tablets because they may have been mislabeled as Liothyronine Sodium 25 mcg.
Aidapak Services, LLC is recalling Hydrochlorothiazide 12.5 mg tablets because they may have been mislabeled as other prescription drugs.
Aidapak Services is recalling Thiothixene 1 mg capsules because they may have been mislabeled as Omega-3 Fatty Acid 1000 mg capsules.
Aidapak Services is recalling Fluconazole 200 mg tablets because they may have been mislabeled as Valsartan or Fluconazole 100 mg.
Aidapak Services, LLC is recalling Acetaminophen chew tablets because they may have been mislabeled as other medications. The repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling Pioglitazone HCL 15 mg tablets because they may have been mislabeled as Doxycycline or Lovastatin.
Aidapak Services is recalling Exemestane 25 mg tablets because they may be mislabeled as Omega-3 Fatty Acid capsules.
Aidapak Services is recalling Lithium Carbonate ER tablets due to a labeling error where they may be mislabeled as other medications.